Pierre Foskett

Denmark Hill
London, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 22 publications

High Frequency of CTNNB1 Variants Associated with Benign and Malignant Liver Tumors in Patients with Congenital Porto-Systemic Shunts.

High Frequency of CTNNB1 Variants Associated with Benign and Malignant Liver Tumors in Patients with Congenital Porto-Systemic Shunts.

Journal: Liver cancer

Published: July 17, 2024

Genetic and functional analysis of chymotrypsin-like protease (CTRL) in chronic pancreatitis.

Genetic and functional analysis of chymotrypsin-like protease (CTRL) in chronic pancreatitis.

Journal: Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.]

Published: September 22, 2023

Guideline Review: European Association for the Study of Liver (EASL) Clinical Practice Guidelines on Haemochromatosis.

Guideline Review: European Association for the Study of Liver (EASL) Clinical Practice Guidelines on Haemochromatosis.

Journal: Journal of clinical and experimental hepatology

Published: August 12, 2022

Clinical phenotype of adult-onset liver disease in patients with variants in ABCB4, ABCB11, and ATP8B1.

Clinical phenotype of adult-onset liver disease in patients with variants in ABCB4, ABCB11, and ATP8B1.

Journal: Hepatology communications

Published: April 07, 2022

ATP7B Genotype and Chronic Liver Disease Treatment Outcomes in Wilson Disease: Worse Survival With Loss-of-Function Variants.

ATP7B Genotype and Chronic Liver Disease Treatment Outcomes in Wilson Disease: Worse Survival With Loss-of-Function Variants.

Journal: Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association

Published: December 13, 2021

Liver Disease and Risk of Hepatocellular Carcinoma in Children With Mutations in TALDO1.

Liver Disease and Risk of Hepatocellular Carcinoma in Children With Mutations in TALDO1.

Journal: Hepatology communications

Published: October 22, 2021

Synonymous mutation in adenosine triphosphatase copper-transporting beta causes enhanced exon skipping in Wilson disease.

Synonymous mutation in adenosine triphosphatase copper-transporting beta causes enhanced exon skipping in Wilson disease.

Journal: Hepatology communications

Published: September 10, 2021

Assessment of quantitative polymerase chain reaction for BCR-ABL1 transcripts in chronic myeloid leukaemia: Are improved outcomes in patients with e14a2 transcripts an artefact of technology?

Assessment of quantitative polymerase chain reaction for BCR-ABL1 transcripts in chronic myeloid leukaemia: Are improved outcomes in patients with e14a2 transcripts an artefact of technology?

Journal: British journal of haematology

Published: September 05, 2021

Study of Acute Liver Failure in Children Using Next Generation Sequencing Technology.

Study of Acute Liver Failure in Children Using Next Generation Sequencing Technology.

Journal: The Journal of pediatrics

Published: February 10, 2021

Cholestasis Due to USP53 Deficiency.

Cholestasis Due to USP53 Deficiency.

Journal: Journal of pediatric gastroenterology and nutrition

Published: October 19, 2020

TKI dose reduction can effectively maintain major molecular remission in patients with chronic myeloid leukaemia.

TKI dose reduction can effectively maintain major molecular remission in patients with chronic myeloid leukaemia.

Journal: British journal of haematology

Published: September 05, 2020

Mutations in Myosin 5B in Children With Early-onset Cholestasis.

Mutations in Myosin 5B in Children With Early-onset Cholestasis.

Journal: Journal of pediatric gastroenterology and nutrition

Published: April 19, 2020

Showing 1-12 of 22

Last Updated: 09/26/2026